The Safety Rates Drug Report

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Drug     Injury     Quarter    

Person who experienced the adverse event (patient)

Event ID CASEID CASEVERSION I F COD EVENT DT MFR DT INIT FDA DT FDA DT REPT COD AUTH NUM MFR NUM MFR SNDR LIT REF AGE AGE COD AGE GRP GNDR COD E SUB WT WT COD REPT DT TO MFR OCCP COD REPORTER COUNTRY OCCR COUNTRY
123846972 12384697 2 F 20160511 20160817 20160519 20160824 EXP US-UCBSA-2016018127 UCB 59.67 YR F Y 0.00000 20160824 CN US US

Drug(s) used by person

Event ID CASEID DRUG SEQ ROLE COD DRUGNAME PROD AI VAL VBM ROUTE DOSE VBM CUM DOSE CHR CUM DOSE UNIT DECHAL RECHAL LOT NUM EXP DT NDA NUM DOSE AMT DOSE UNIT DOSE FORM DOSE FREQ
123846972 12384697 1 PS CIMZIA CERTOLIZUMAB PEGOL 1 Subcutaneous STRENGTH- 200 MG IN PRE FILLED SYRINGE, 200 MG, EV 2 WEEKS(QOW) NDC#50474-710-79 125160 200 MG SOLUTION FOR INJECTION QOW
123846972 12384697 2 C PERCOCET ACETAMINOPHENOXYCODONE HYDROCHLORIDE 1 UNK U 0
123846972 12384697 3 C LIDODERM LIDOCAINE 1 U 0 PATCH
123846972 12384697 4 C ARAVA LEFLUNOMIDE 1 UNK U 0
123846972 12384697 5 C METHOTREXATE. METHOTREXATE 1 U 0

Indications of drugs used

Event ID CASEID INDI DRUG SEQ INDI PT
123846972 12384697 1 Rheumatoid arthritis
123846972 12384697 2 Pain
123846972 12384697 3 Pain
123846972 12384697 4 Product used for unknown indication
123846972 12384697 5 Product used for unknown indication

Outcome of event

Event ID CASEID OUTC COD
123846972 12384697 OT

Reactions reported

Event ID CASEID DRUG REC ACT PT
123846972 12384697 Bronchitis
123846972 12384697 Feeling abnormal
123846972 12384697 Hypertension
123846972 12384697 Incorrect product storage
123846972 12384697 Lung disorder
123846972 12384697 Nodule
123846972 12384697 Pain
123846972 12384697 Pneumonia
123846972 12384697 Sinusitis

Reporting Sources (this data is often not reported and may therefore be missing here)

no results found

Therapies reported

Event ID CASEID DSG DRUG SEQ START DT END DT DUR DUR COD
123846972 12384697 1 201503 0